Zobrazeno 1 - 10
of 317
pro vyhledávání: '"Sonoko, Misawa"'
Autor:
Arata Ishii, Shokichi Tsukamoto, Naoya Mimura, Yurie Miyamoto-Nagai, Yusuke Isshiki, Shinichiro Matsui, Sanshiro Nakao, Asuka Shibamiya, Yutaro Hino, Kensuke Kayamori, Nagisa Oshima-Hasegawa, Tomoya Muto, Yusuke Takeda, Tomoki Suichi, Sonoko Misawa, Chikako Ohwada, Koutaro Yokote, Satoshi Kuwabara, Chiaki Nakaseko, Hiroyuki Takamatsu, Emiko Sakaida
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-9 (2024)
Abstract POEMS syndrome (polyneuropathy, organomegaly, endocrinopathy, monoclonal protein [M-protein], and skin changes) is a rare systemic disorder characterized by various symptoms caused by underlying plasma cell (PC) dyscrasia. Detection of monoc
Externí odkaz:
https://doaj.org/article/9b8f610b006b45589b8f86626a22aab6
Autor:
Sonoko Misawa, Tadamichi Denda, Sho Kodama, Takuji Suzuki, Yoichi Naito, Takahiro Kogawa, Mamoru Takada, Tomoki Suichi, Kazuhito Shiosakai, Satoshi Kuwabara, on behalf of the MiroCIP study group
Publikováno v:
BMC Cancer, Vol 23, Iss 1, Pp 1-11 (2023)
Abstract Background Chemotherapy-induced peripheral neuropathy (CIPN) is a painful, dose-limiting adverse effect of commonly used chemotherapeutic agents. The purpose of this exploratory study was to evaluate the efficacy and safety of mirogabalin in
Externí odkaz:
https://doaj.org/article/5c5d7bed96f94e5a8e4f6cacca56729a
Autor:
Hirotaka Yokouchi, Daisuke Nagasato, Yoshinori Mitamura, Mariko Egawa, Hitoshi Tabuchi, Sonoko Misawa, Satoshi Kuwabara, Takayuki Baba
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-8 (2023)
Abstract A higher serum vascular endothelial growth factor (VEGF) level can cause choroidal thickening in the choroid of patients with polyneuropathy, organomegaly, endocrinopathy, monoclonal gammopathy, and skin changes (POEMS) syndrome. We aimed to
Externí odkaz:
https://doaj.org/article/48a4d87d8e7345be9da45008e67e9935
Autor:
Yo-ichi Suzuki, Kazumoto Shibuya, Sonoko Misawa, Tomoki Suichi, Atsuko Tsuneyama, Yuta Kojima, Keigo Nakamura, Hiroki Kano, Mario Prado, Satoshi Kuwabara
Publikováno v:
BMC Neurology, Vol 22, Iss 1, Pp 1-7 (2022)
Abstract Background and purpose Muscle ultrasonography has been increasingly recognized as a useful tool for detection of fasciculations. Separately, concordance between dominant hand and onset side has been reported in amyotrophic lateral sclerosis
Externí odkaz:
https://doaj.org/article/83be9b11d94c48558ae479d2d40ff45f
Autor:
Atsuko Tsuneyama, Kazumoto Shibuya, Sonoko Misawa, Yo-ichi Suzuki, Tomoki Suichi, Yuta Kojima, Keigo Nakamura, Hiroki Kano, Mario J. Prado, Satoshi Kuwabara
Publikováno v:
Clinical Neurophysiology Practice, Vol 7, Iss , Pp 71-77 (2022)
Objective: Fatigue is a major disabling problem in patients with neuromuscular disorders. Both nerve demyelination and increased axonal branching associated with collateral sprouting reduce the safety factor for impulse transmission and could cause a
Externí odkaz:
https://doaj.org/article/4541f77ff04e41cb8713b89f89e7a613
Autor:
Yusuke Isshiki, Motohiko Oshima, Naoya Mimura, Kensuke Kayamori, Yurie Miyamoto-Nagai, Masahide Seki, Yaeko Nakajima-Takagi, Takashi Kanamori, Eisuke Iwamoto, Tomoya Muto, Shokichi Tsukamoto, Yusuke Takeda, Chikako Ohwada, Sonoko Misawa, Jun-ichiro Ikeda, Masashi Sanada, Satoshi Kuwabara, Yutaka Suzuki, Emiko Sakaida, Chiaki Nakaseko, Atsushi Iwama
Publikováno v:
JCI Insight, Vol 7, Iss 20 (2022)
POEMS syndrome is a rare monoclonal plasma cell disorder, with unique symptoms distinct from those of other plasma cell neoplasms, including high serum VEGF levels. Because the prospective isolation of POEMS clones has not yet been successful, their
Externí odkaz:
https://doaj.org/article/1465a2b380054f029fc2853ac8d0fd0e
Autor:
Atsuhiko Sugiyama, Hajime Yokota, Sonoko Misawa, Hiroki Mukai, Yukari Sekiguchi, Kyosuke Koide, Tomoki Suichi, Jun Matsushima, Takashi Kishimoto, Zen-ichi Tanei, Yuko Saito, Shoichi Ito, Satoshi Kuwabara
Publikováno v:
BMC Neurology, Vol 21, Iss 1, Pp 1-9 (2021)
Abstract Background This study aimed to investigate the frequency and risk factors for cerebral artery stenosis and occlusion in patients with polyneuropathy, organomegaly, endocrinopathy, M-protein, and skin changes (POEMS) syndrome. Methods We revi
Externí odkaz:
https://doaj.org/article/fcf0bfbd14e84367bc0d68aed341c2ef
Autor:
Yuya Aotsuka, Sonoko Misawa, Tomoki Suichi, Kazumoto Shibuya, Keigo Nakamura, Hiroki Kano, Ryo Otani, Marie Morooka, Moeko Ogushi, Kengo Nagashima, Yasunori Sato, Nagato Kuriyama, Satoshi Kuwabara
Publikováno v:
Neurology; 3/26/2024, Vol. 102 Issue 6, p1-11, 11p
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 13, Iss 1, Pp 1-17 (2018)
Abstract Hereditary ATTR (ATTRm) amyloidosis (also called transthyretin-type familial amyloid polyneuropathy [ATTR-FAP]) is an autosomal-dominant, adult-onset, rare systemic disorder predominantly characterized by irreversible, progressive, and persi
Externí odkaz:
https://doaj.org/article/75984d050ccf49a895d79b23b6c4d974
Autor:
Tomoki, Suichi, Sonoko, Misawa, Yukari, Sekiguchi, Kazumoto, Shibuya, Keigo, Nakamura, Hiroki, Kano, Yuya, Aotsuka, Ryo, Otani, Marie, Morooka, Shokichi, Tsukamoto, Yusuke, Takeda, Naoya, Mimura, Chikako, Ohwada, Emiko, Sakaida, Satoshi, Kuwabara
Publikováno v:
Internal Medicine. 61:2567-2572
Objective Immunomodulatory drugs and proteasome inhibitors are therapeutic options for polyneuropathy, organomegaly, endocrinopathy, monoclonal gammopathy, and skin changes (POEMS) syndrome. This study aimed to evaluate the efficacy and safety of the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7368f9cef0b021f24d5ae31097131714
https://doi.org/10.2169/internalmedicine.8786-21
https://doi.org/10.2169/internalmedicine.8786-21